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Scientific Medical Writer Jobs

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Scientific and Medical Writer
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Join AB Science in Paris as a Scientific and Medical Writer. You will author key regulatory documents, including clinical study reports and marketing authorisation applications (eCTD). This permanent role requires a biomedical postgraduate degree, fluency in English, and proven writing skills. Ma...
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France , Paris
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Not provided
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AB SCIENCE
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Until further notice
Medical Writer, Scientific Communications
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Join Vaniam Group as a Medical Writer for Scientific Communications in a 100% remote US role. Utilize your PhD/MD/PharmD and 1+ years of agency/pharma experience to develop high-quality scientific content. Enjoy a supportive culture, professional growth, and comprehensive benefits while collabora...
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United States
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70000.00 - 85000.00 USD / Year
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Vaniam Group
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Until further notice
Scientific Medical Writer
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Join our mission-driven team in Copenhagen as a Scientific Medical Writer. You will translate complex research into high-impact manuscripts, regulatory documents, and medical communications. A PhD in life sciences and proven publication experience are essential. Make a meaningful impact in rare b...
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Denmark , Københavns Kommune
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Not provided
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Life Science Talent
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Until further notice
Explore a world of opportunity in scientific medical writer jobs, a dynamic and intellectually rewarding profession at the heart of healthcare innovation. Scientific Medical Writers are specialized communicators who translate complex scientific and clinical data into clear, accurate, and compelling documents that drive drug development, inform regulatory decisions, and advance medical knowledge. They serve as an essential bridge between research scientists, clinical development teams, regulatory agencies, and the broader medical community. Professionals in this field are responsible for authoring a wide array of critical documents throughout a product's lifecycle. Common responsibilities include preparing manuscripts for peer-reviewed journals, clinical study reports (CSRs), protocols, and investigator brochures (IBs). A significant portion of the role involves crafting regulatory submissions such as Investigational New Drug (IND) applications, Clinical Trial Applications (CTAs), and Marketing Authorisation Applications (MAAs). Beyond regulatory needs, these writers develop content for scientific conferences (abstracts, posters, presentations), create medical education materials, and support Medical Affairs by producing scientifically accurate communications for healthcare professionals, advisory boards, and key opinion leader (KOL) engagements. The role demands meticulous project management, as writers typically juggle multiple documents with strict deadlines, ensuring all content adheres to rigorous ethical, compliance, and industry-standard guidelines. Typical requirements for scientific medical writer jobs include an advanced degree (Ph.D., Pharm.D., or M.D.) in a life science discipline such as biomedical sciences, pharmacology, or immunology. Demonstrated experience in scientific writing, often evidenced by peer-reviewed publications, is paramount. A strong understanding of clinical research methodology, biostatistics, and the regulatory landscape (ICH, GCP) is essential. The ideal candidate possesses exceptional writing and editing skills with the ability to distill intricate data for varied audiences, from regulatory experts to clinicians. Success in these roles hinges on a sharp attention to detail, superior organizational skills, and the ability to collaborate effectively with cross-functional teams in research, clinical development, and regulatory affairs. For those with a passion for science and precision in language, scientific medical writer jobs offer a critical and fulfilling career path shaping the future of medicine.

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